Reveal Robust(显示稳健)研究综述
Reveal Robust 显示稳健 - Conclusions Our findings, replicated across two independent cohorts, reveal robust and neurobiologically interpretable brain features that detect ASD and predict core phenotypic features of ASD, and have the potential to transform our understanding of the etiology and treatment of the disorder. [1] Collectively, our results reveal robust exonuclease activity of S. [2] Empirical results reveal robustness of the proposed technique. [3] The results reveal robust vessel segmentation and AV classification. [4] Highlights We developed a novel method by which human fibroblasts are reprogrammed until the maturation phase of iPSCs and are then returned to fibroblast identity DNA methylation memory in fibroblast enhancers may allow recovery of cell identity when fibroblast gene expression programmes are already extinct Molecular measures of ageing including transcriptome and DNA methylation clocks and H3K9me3 levels reveal robust and substantial rejuvenation Functional rejuvenation of fibroblasts by MPTR is suggested by reacquisition of youthful levels of collagen proteins. [5] Furthermore, longitudinal analyses reveal robust S‐protein‐driven inflammasome activation in macrophages isolated from convalescent COVID‐19 patients, which correlates with distinct epigenetic and gene expression signatures suggesting innate immune memory after recovery from COVID‐19. [6] Our results reveal robust, long-lasting benefits induced by FBA in VPL, and have translational implications for improving generalization of training protocols in visual rehabilitation. [7] Our results reveal robust, long-lasting benefits induced by FBA in VPL, and have translational implications for improving generalization of training protocols in visual rehabilitation. [8] Monte Carlo simulations reveal robust improvements over standard methods in finite samples. [9] 17films, however, reveal robust superconductivity even with thickness d ≈ 2 nm. [10] Our findings reveal robust changes in placentation during maternal iron deficiency, which could contribute to the increased risk of fetal distress in these pregnancies. [11] Analyses reveal robust brain activations that are consistent with the published literature, vary across fMRI tasks/contrasts and slightly correlate with individual behavioral performance on the tasks. [12] Our data reveal robust, widespread translation of non-canonical transcripts and point toward different translation initiation mechanisms compared to canonical Shine-Dalgarno transcripts. [13] These findings indicate that microglia are physiologically more important than ever thought to reveal robust brain functions. [14] Studies on subject‐derived osteoclasts from peripheral blood mononuclear cells did not reveal robust defects in mature osteoclast formation or resorptive activity. [15] Furthermore, simulations results also reveal robust performance in high mobility scenarios. [16]结论 我们的研究结果在两个独立的队列中重复，揭示了检测 ASD 和预测 ASD 核心表型特征的强大且神经生物学可解释的大脑特征，并有可能改变我们对疾病病因和治疗的理解。 [1] 总的来说，我们的结果揭示了 S. [2] 实证结果揭示了所提出技术的稳健性。 [3] 结果揭示了强大的血管分割和 AV 分类。 [4] 亮点 我们开发了一种新方法，通过该方法将人类成纤维细胞重新编程，直到 iPSC 成熟阶段，然后返回成纤维细胞身份 成纤维细胞增强剂中的 DNA 甲基化记忆可能允许在成纤维细胞基因表达程序已经灭绝时恢复细胞身份 衰老的分子测量，包括转录组和 DNA 甲基化时钟以及 H3K9me3 水平揭示了强大而显着的年轻化功能 MPTR 对成纤维细胞的功能性年轻化是通过重新获得年轻水平的胶原蛋白来实现的。 [5] 此外，纵向分析揭示了从恢复期 COVID-19 患者中分离出的巨噬细胞中 S 蛋白驱动的炎症小体强烈激活，这与不同的表观遗传和基因表达特征相关，表明从 COVID-19 恢复后的先天免疫记忆。 [6] 我们的结果揭示了 FBA 在 VPL 中产生的强大、持久的益处，并且对改进视觉康复训练方案的泛化具有转化意义。 [7] 我们的结果揭示了 FBA 在 VPL 中产生的强大、持久的益处，并且对改进视觉康复训练方案的泛化具有转化意义。 [8] 蒙特卡罗模拟揭示了有限样本中标准方法的稳健改进。 [9] 然而，即使厚度 d ≈ 2 nm，17 薄膜也显示出强大的超导性。 [10] 我们的研究结果揭示了母体缺铁期间胎盘的强烈变化，这可能导致这些妊娠中胎儿窘迫的风险增加。 [11] 分析揭示了与已发表的文献一致的强大的大脑激活，在 fMRI 任务/对比中有所不同，并且与任务中的个人行为表现略有相关。 [12] 我们的数据揭示了非规范转录本的稳健、广泛的翻译，并指出了与规范 Shine-Dalgarno 转录本相比不同的翻译起始机制。 [13] 这些发现表明，小胶质细胞在生理上比以往任何时候都更重要，可以揭示强大的大脑功能。 [14] 对来自外周血单个核细胞的受试者来源的破骨细胞的研究并未揭示成熟破骨细胞形成或吸收活性的严重缺陷。 [15] 此外，模拟结果还揭示了在高移动性场景中的稳健性能。 [16]
Result Reveal Robust
Collectively, our results reveal robust exonuclease activity of S. [1] Empirical results reveal robustness of the proposed technique. [2] The results reveal robust vessel segmentation and AV classification. [3] Our results reveal robust, long-lasting benefits induced by FBA in VPL, and have translational implications for improving generalization of training protocols in visual rehabilitation. [4] Our results reveal robust, long-lasting benefits induced by FBA in VPL, and have translational implications for improving generalization of training protocols in visual rehabilitation. [5]总的来说，我们的结果揭示了 S. [1] 实证结果揭示了所提出技术的稳健性。 [2] 结果揭示了强大的血管分割和 AV 分类。 [3] 我们的结果揭示了 FBA 在 VPL 中产生的强大、持久的益处，并且对改进视觉康复训练方案的泛化具有转化意义。 [4] 我们的结果揭示了 FBA 在 VPL 中产生的强大、持久的益处，并且对改进视觉康复训练方案的泛化具有转化意义。 [5]
Analysis Reveal Robust
Furthermore, longitudinal analyses reveal robust S‐protein‐driven inflammasome activation in macrophages isolated from convalescent COVID‐19 patients, which correlates with distinct epigenetic and gene expression signatures suggesting innate immune memory after recovery from COVID‐19. [1] Analyses reveal robust brain activations that are consistent with the published literature, vary across fMRI tasks/contrasts and slightly correlate with individual behavioral performance on the tasks. [2]此外，纵向分析揭示了从恢复期 COVID-19 患者中分离出的巨噬细胞中 S 蛋白驱动的炎症小体强烈激活，这与不同的表观遗传和基因表达特征相关，表明从 COVID-19 恢复后的先天免疫记忆。 [1] 分析揭示了与已发表的文献一致的强大的大脑激活，在 fMRI 任务/对比中有所不同，并且与任务中的个人行为表现略有相关。 [2]
reveal robust brain
Analyses reveal robust brain activations that are consistent with the published literature, vary across fMRI tasks/contrasts and slightly correlate with individual behavioral performance on the tasks. [1] These findings indicate that microglia are physiologically more important than ever thought to reveal robust brain functions. [2]分析揭示了与已发表的文献一致的强大的大脑激活，在 fMRI 任务/对比中有所不同，并且与任务中的个人行为表现略有相关。 [1] 这些发现表明，小胶质细胞在生理上比以往任何时候都更重要，可以揭示强大的大脑功能。 [2]